Cryo-EM: A Unique Tool for the Visualization of Macromolecular Complexity

被引:253
|
作者
Nogales, Eva [1 ,2 ,3 ]
Scheres, Sjors H. W. [4 ]
机构
[1] Univ Calif Berkeley, Mol & Cell Biol Dept, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Life Sci, Berkeley, CA 94720 USA
[4] MRC Lab Mol Biol, Cambridge CB2 0QH, England
基金
英国医学研究理事会;
关键词
RNA-POLYMERASE-II; TRANSMISSION ELECTRON-MICROSCOPY; LIKELIHOOD-BASED CLASSIFICATION; SINGLE-PARTICLE ANALYSIS; GAMMA-SECRETASE COMPLEX; LARGE RIBOSOMAL-SUBUNIT; BEAM-INDUCED MOTION; ALPHA-BETA-TUBULIN; CRYOELECTRON MICROSCOPY; ANGSTROM RESOLUTION;
D O I
10.1016/j.molcel.2015.02.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
3D cryo-electron microscopy (cryo-EM) is an expanding structural biology technique that has recently undergone a quantum leap progression in its achievable resolution and its applicability to the study of challenging biological systems. Because crystallization is not required, only small amounts of sample are needed, and because images can be classified in a computer, the technique has the potential to deal with compositional and conformational mixtures. Therefore, cryo-EM can be used to investigate complete and fully functional macromolecular complexes in different functional states, providing a richness of biological insight. In this review, we underlie some of the principles behind the cryo-EM methodology of single particle analysis and discuss some recent results of its application to challenging systems of paramount biological importance. We place special emphasis on new methodological developments that are leading to an explosion of new studies, many of which are reaching resolutions that could only be dreamed of just a couple of years ago.
引用
收藏
页码:677 / 689
页数:13
相关论文
共 50 条
  • [41] Fusion of DARPin to Aldolase Enables Visualization of Small Protein by Cryo-EM
    Yao, Qing
    Weaver, Sara J.
    Mock, Jee-Young
    Jensen, Grant J.
    STRUCTURE, 2019, 27 (07) : 1148 - +
  • [42] Unraveling the complexity of amyloid polymorphism using gold nanoparticles and cryo-EM
    Cendrowska, Urszula
    Silva, Paulo Jacob
    Ait-Bouziad, Nadine
    Mueller, Marie
    Guven, Zekiye Pelin
    Vieweg, Sophie
    Chiki, Anass
    Radamaker, Lynn
    Kumar, Senthil T.
    Faendrich, Marcus
    Tavanti, Francesco
    Menziani, Maria Cristina
    Alexander-Katz, Alfredo
    Stellacci, Francesco
    Lashuel, Hilal A.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (12) : 6866 - 6874
  • [43] Cryo-EM research in India
    Shukla, Arun K.
    Banerjee, Manidipa
    Singh, Appu K.
    Penmatsa, Aravind
    Dutta, Somnath
    Anand, Ruchi
    Sirajuddin, Minhajuddin
    STRUCTURE, 2024, 32 (02) : 113 - 119
  • [44] Dynamincs of Dynamin by CRYO-EM
    Kundu, Nidhi
    Jimah, John
    Stanton, Abigail
    Chan, Lieza M.
    Dandey, Venkata P.
    Potter, Clinton S.
    Carragher, Bridget
    Hinshaw, Jenny E.
    BIOPHYSICAL JOURNAL, 2020, 118 (03) : 403A - 403A
  • [45] Cryo-EM at ACA 2022
    Subramaniam, Sriram
    Kotecha, Abhay
    Davis, Joseph H.
    IUCRJ, 2022, 9 : 713 - 714
  • [46] A dynamic direction for cryo-EM
    Allison Doerr
    Nature Methods, 2022, 19 : 29 - 29
  • [47] Cryo-EM: beyond the microscope
    Earl, Lesley A.
    Falconieri, Veronica
    Milne, Jacqueline L. S.
    Subramaniam, Sriram
    CURRENT OPINION IN STRUCTURAL BIOLOGY, 2017, 46 : 71 - 78
  • [48] Cryo-EM for protein discovery
    Ullrich, Florian
    NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2021, 28 (12) : 958 - 958
  • [49] MULTIPARTICLE CRYO-EM OF RIBOSOMES
    Loerke, Justus
    Giesebrecht, Jan
    Spahn, Christian M. T.
    METHODS IN ENZYMOLOGY, VOL 483: CRYO-EM, PART C: ANALYSES, INTERPRETATION, AND CASE STUDIES, 2010, 483 : 161 - 177
  • [50] Scratching the itch with cryo-EM
    Maharana, Jagannath
    Sarma, Parishmita
    Shukla, Arun K.
    NATURE CHEMICAL BIOLOGY, 2022, 18 (03) : 242 - 243